Publications by authors named "Troy A Becker"

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Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848.
Magdalena Koczkowska, Yunjia Chen, Tom Callens, Alicia Gomes, Angela Sharp, Troy A Becker

Am J Hum Genet· January 2018

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Gain-of-Function Mutations in RARB Cause Intellectual Disability with Progressive Motor Impairment.
Myriam Srour, Véronique Caron, Toni Pearson, Sarah B Nielsen, Sébastien Lévesque, Troy A Becker

Hum Mutat· August 2016

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Inherited 14q duplication and 21q deletion: a rare adjacent-2 segregation in multiple family members.
Bhavana J Dave, Ann Haskins Olney, Dianna H Zaleski, Diane L Pickering, Troy A Becker

Am J Med Genet A· October 2009

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A patient with an interstitial duplication of chromosome 5p11-p13.3 further confirming a critical region for 5p duplication syndrome.
Melissa L Loscalzo, Troy A Becker, Maxine Sutcliffe

Eur J Med Genet· June 2008

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